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| Structural eye disease v0.76 | CNGB1 | Nicola Ragge reviewed gene: CNGB1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 45, 613767; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CNGB1 | Ivone Leong reviewed gene: CNGB1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 45, 613767; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CNGB1 |
Ivone Leong Source NHS GMS was added to CNGB1. Mode of inheritance for gene CNGB1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 45, 613767 for gene: CNGB1 |
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| Structural eye disease v0.2 | CNGB1 |
Ellen McDonagh gene: CNGB1 was added gene: CNGB1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CNGB1 was set to Phenotypes for gene: CNGB1 were set to Eye Disorders |
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